Elisabeth Young

Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres

Ashok Vellodi, Elisabeth Young, Alan Cooper et al. · Archives of Disease in Childhood · 1997 · 207 citations · Full text

Hla Identical Relative, Transplantation, Marrow Transplantation +11

Pathologic gene expression in Gaucher disease: up-regulation of cysteine proteinases including osteoclastic cathepsin K

Mary Teresa Moran, J. Paul Schofield, Alison R. Hayman et al. · Blood · 2000 · 153 citations

Treatment of Fabry disease with different dosing regimens of agalsidase: Effects on antibody formation and GL-3

Anouk C. Vedder, Frank Breunig, Wilma E. Donker‐Koopman et al. · Molecular Genetics and Metabolism · 2008 · 134 citations

Fabry Disease, Immunology, Pathology +2

Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations

Cathy Meaney, Gavin Greenland, Vanessa M. Adams et al. · Human Genetics · 2001 · 128 citations

Vitro Expression, Mutational Analysis, Mucopolysaccharidosis Type +9

The Neurological Complications of Anderson—Fabry Disease (α-Galactosidase A Deficiency)—Investigation of Symptomatic and Presymptomatic Patients

Stephen H. Morgan, Peter Rudge, Stuart Smith et al. · QJM · 1990 · 108 citations